DIHEXA 10mg

DIHEXA 10mg

Note:
  • USA MADE 2-7 days delivery
  • International 5-20 days delivery
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Product Overview

A fundamental standard in neurological and cognitive performance research dictates that exploring advanced neurotrophic agents requires complete structural integrity and verified chemical purity. The Dihexa formulation addresses these demanding benchmarks, serving as a highly purified synthetic peptide derivative developed for precise in vitro and in vivo laboratory modeling. Each vial provides 10mg of pure Dihexa, stabilized as a vacuum freeze-dried (lyophilized) powder maintaining a verified purity profile of greater than 98%.

Dihexa (also known as N-hexanoic-Tyr-Ile-Ahx-NH2) is an oligopeptide drug variant derived from angiotensin IV (AngIV). Characterized by a molecular weight of 532.7 g/mol and a chemical formula of C27H44N4O6, this small molecule possesses a distinct structural stability asset over standard endogenous neurotrophins like brain-derived neurotrophic factor (BDNF). Because of its minimized structural framework, Dihexa exhibits exceptional clearance and blood-brain barrier permeability kinetics in laboratory models, allowing it to penetrate cellular microenvironments rapidly and demonstrate high bioactivity without the rapid metabolic breakdown typical of heavy native proteins.

Operating primarily as a potent hepatocyte growth factor (HGF) modulator, Dihexa binds with high affinity to the native HGF ligand. This binding interaction facilitates the dimerization and subsequent activation of c-Met, the receptor tyrosine kinase specific to HGF. Activation of the HGF/c-Met signaling pathway triggers downstream intracellular cascades, notably the mitogen-activated protein kinase (MAPK) and phosphoinositide 3-kinase/Akt (PI3K/Akt) pathways. Documented research demonstrates that Dihexa actively drives spinogenesis, induces dendritic arborization, and enhances synaptic plasticity. These diverse mechanisms allow for the precise investigation of synaptogenesis biochemistry, neurodegenerative models, and cellular longevity within controlled laboratory settings.

Product Specifications

  • Form: Lyophilized (vacuum freeze-dried) powder
  • Quantity: 10mg per vial
  • Purity: Greater than 98% (verified by HPLC analysis)
  • Molecular Weight: 532.7 g/mol
  • Primary Target: HGF/c-Met Receptor Complex Agonist
  • Primary Research Focus: Synaptogenesis Induction, Spinogenesis Kinetics, and Neuroprotective Pathways

Container Specifications

The physical attributes of the storage vessel directly impact the shelf life of the compound. All research environments should utilize clean, chemically inert containers. Glass vials provide the highest level of protection against gas permeability and chemical interaction, though high-density polypropylene tubes serve as a valid alternative. Keep all stored peptides away from automatic frost-free freezers, as their internal defrost cycles create regular temperature swings that compromise peptide longevity.

Storage and Handling Protocols

Preserving the biological utility of a high-purity neurotrophic peptide requires strict adherence to precise environmental controls. Because the specific oligopeptide structure remains vulnerable to thermal, moisture-driven, and atmospheric degradation, researchers must follow standardized handling protocols to prevent structural breakdown.

Lyophilized Powder Preservation

Unopened, lyophilized vials must be kept in long-term cold storage at a stable temperature of -20°C. For extended storage timelines exceeding one year, maintaining a temperature of -80°C is highly recommended to completely arrest baseline molecular degradation. Vials should remain housed in sealed, light-shielded containers to prevent degradation from ultraviolet exposure and atmospheric moisture.

Before opening a vial or introducing a reconstitution solvent, allow the container to sit at room temperature until it fully equilibrates. Skipping this step introduces a substantial risk of moisture condensation forming on the cold powder, which immediately accelerates enzymatic breakdown.

Properly stored at -20°C, the lyophilized powder remains stable and viable for a period of 2 to 4 years.

For optimal preservation, utilize airtight glass vials equipped with PTFE-lined caps. If a vial is opened to remove fractional quantities, the remaining headspace should be flushed with an inert gas like dry nitrogen or argon before resealing to minimize oxidative risk across the short peptide structure.

Reconstituted Solution Stability

Once transitioned into a liquid state, the peptide becomes significantly more fragile. Reconstituted Dihexa solutions must be kept under continuous refrigeration at 2-8°C and should be completely utilized within 30 days. If your experimental timeline requires keeping the liquid compound past this threshold, divide the freshly mixed solution into single-use aliquots immediately after reconstitution and freeze them at -20°C or -80°C.

To maintain maximum stability, employ sterile, neutral buffers or sterile water. Repeated freeze-thaw cycles must be strictly avoided, as the physical stress of phase changes causes structural shearing of the peptide architecture.

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At PeptideHubs, scientific integrity and product reliability are at the core of everything we do. Each compound is manufactured and tested under strict quality control protocols to ensure consistency, purity, and performance for research applications.

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